The rat intervertebral disk degeneration pain model: relationships between biological and structural alterations and pain

被引:68
作者
Kim, Jae-Sung [1 ]
Kroin, Jeffrey S. [2 ]
Li, Xin [1 ]
An, Howard S. [3 ]
Buvanendran, Asokumar [2 ]
Yan, Dongyao [1 ]
Tuman, Kenneth J. [2 ]
van Wijnen, Andre J. [4 ]
Chen, Di [1 ]
Im, Hee-Jeong [1 ,3 ,5 ,6 ]
机构
[1] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Anesthesiol, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
[4] Univ Massachusetts, Dept Cell Biol, Worcester, MA 01655 USA
[5] Rush Univ, Med Ctr, Dept Internal Med, Rheumatol Sect, Chicago, IL 60612 USA
[6] Univ Illinois, Dept Bioengn, Chicago, IL 60607 USA
关键词
lumbar disk degeneration; pain pathway; chronic back pain; animal model; drug test; pain intervention; LOW-BACK-PAIN; GENE-RELATED PEPTIDE; DORSAL-ROOT GANGLIA; NEUROPATHIC PAIN; NEUROTROPHIC FACTORS; POSTOPERATIVE PAIN; SENSORY NEURONS; NEEDLE PUNCTURE; PRESSURE PAIN; UP-REGULATION;
D O I
10.1186/ar3485
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Introduction: Degeneration of the interverterbral disk is as a cause of low-back pain is increasing. To gain insight into relationships between biological processes, structural alterations and behavioral pain, we created an animal model in rats. Methods: Disk degeneration was induced by removal of the nucleus pulposus (NP) from the lumbar disks (L4/L5 and L5/L6) of Sprague Dawley rats using a 0.5-mm-diameter microsurgical drill. The degree of primary hyperalgesia was assessed by using an algometer to measure pain upon external pressure on injured lumbar disks. Biochemical and histological assessments and radiographs of injured disks were used for evaluation. We investigated therapeutic modulation of chronic pain by administering pharmaceutical drugs in this animal model. Results: After removal of the NP, pressure hyperalgesia developed over the lower back. Nine weeks after surgery we observed damaged or degenerated disks with proteoglycan loss and narrowing of disk height. These biological and structural changes in disks were closely related to the sustained pain hyperalgesia. A high dose of morphine (6.7 mg/kg) resulted in effective pain relief. However, high doses of pregabalin (20 mg/kg), a drug that has been used for treatment of chronic neuropathic pain, as well as the anti-inflammatory drugs celecoxib (50 mg/kg; a selective inhibitor of cyclooxygenase 2 (COX-2)) and ketorolac (20 mg/kg; an inhibitor of COX-1 and COX-2), did not have significant antihyperalgesic effects in our disk injury animal model. Conclusions: Although similarities in gene expression profiles suggest potential overlap in chronic pain pathways linked to disk injury or neuropathy, drug-testing results suggest that pain pathways linked to these two chronic pain conditions are mechanistically distinct. Our findings provide a foundation for future research on new therapeutic interventions that can lead to improvements in the treatment of patients with back pain due to disk degeneration.
引用
收藏
页数:11
相关论文
共 32 条
[1]
Surgically induced osteoarthritis in the rat results in the development of both osteoarthritis-like joint pain and secondary hyperalgesia [J].
Bove, S. E. ;
Laemont, K. D. ;
Brooker, R. M. ;
Osborn, M. N. ;
Sanchez, B. M. ;
Guzman, R. E. ;
Hook, K. E. ;
Juneau, P. L. ;
Connor, J. R. ;
Kilgore, K. S. .
OSTEOARTHRITIS AND CARTILAGE, 2006, 14 (10) :1041-1048
[2]
STATISTICAL-METHODS FOR ASSESSING OBSERVER VARIABILITY IN CLINICAL MEASURES [J].
BRENNAN, P ;
SILMAN, A .
BMJ-BRITISH MEDICAL JOURNAL, 1992, 304 (6840) :1491-1494
[3]
QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63
[4]
Acute and chronic effects of neurotrophic factors BDNF and GDNF on responses mediated by thermo-sensitive TRP channels in cultured rat dorsal root ganglion neurons [J].
Ciobanu, Cristian ;
Reid, Gordon ;
Babes, Alexandru .
BRAIN RESEARCH, 2009, 1284 :54-67
[5]
The influence of non-specific low back pain on pressure pain thresholds and disability [J].
Farasyn, A ;
Meeusen, R .
EUROPEAN JOURNAL OF PAIN, 2005, 9 (04) :375-381
[6]
Pain related behaviour in two models of osteoarthritis in the rat knee [J].
Fernihough, J ;
Gentry, C ;
Malcangio, M ;
Fox, A ;
Rediske, J ;
Pellas, T ;
Kidd, B ;
Bevan, S ;
Winter, J .
PAIN, 2004, 112 (1-2) :83-93
[7]
Detection of static and dynamic components of mechanical allodynia in rat models of neuropathic pain: are they signalled by distinct primary sensory neurones? [J].
Field, MJ ;
Bramwell, S ;
Hughes, J ;
Singh, L .
PAIN, 1999, 83 (02) :303-311
[8]
Mouse strains that lack spinal dynorphin upregulation after peripheral nerve injury do not develop neuropathic pain [J].
Gardell, LR ;
Ibrahim, M ;
Wang, R ;
Wang, Z ;
Ossipov, MH ;
Malan, TP ;
Porreca, F ;
Lai, J .
NEUROSCIENCE, 2004, 123 (01) :43-52
[9]
A comparison of pressure pain detection thresholds in people with chronic low back pain and volunteers without pain [J].
Giesbrecht, RJS ;
Battié, MC .
PHYSICAL THERAPY, 2005, 85 (10) :1085-1092
[10]
Discogenic pain [J].
Hurri, H ;
Karppinen, J .
PAIN, 2004, 112 (03) :225-228